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VIVERE BOVINE PERICARDIUM VALVE - Indonesia BPOM Medical Device Registration

VIVERE BOVINE PERICARDIUM VALVE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30504320172. The device is manufactured by BRAILE BIOMร‰DICA INDUSTRIA, COMERCIO E REPRESENTACOES LTDA from Brazil, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MULTIDAYA MEDIKA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : D
VIVERE BOVINE PERICARDIUM VALVE
Analysis ID: AKL 30504320172

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Brazil

Authorized Representative

MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Jul 12, 2023

Expiry Date

Jul 23, 2026

Product Type

Surgical Cardiology Equipment

Aortic Heart Valve, More Than Minimally Manipulated Allograft

Non Electromedic Sterile

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